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TSPO PET in the Evaluation of Neuroinflammation in Patients with Multiple System Atrophy

TSPO PET in the Evaluation of Neuroinflammation in Patients with Multiple System Atrophy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06890390
Enrollment
90
Registered
2025-03-24
Start date
2024-09-14
Completion date
2026-03-31
Last updated
2025-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple System Atrophy - Cerebellar Subtype (MSA-C), Multiple System Atrophy - Parkinsonian Subtype (MSA-P)

Keywords

Multiple System Atrophy, PETCT, TSPO

Brief summary

The aim of this study was to apply PET/MR techniques targeting TSPO to explore the temporal and spatial alterations characterizing neuroinflammation in MSA patients, and to assess its value as a biomarker for diagnostic typing, disease severity, and prognosis of MSA disease.

Interventions

None listed

Sponsors

Min Zhao,MD
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
35 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Age\> 35 years old, gender is not limited; * Clinically confirmed MSA and clinically probable MSA according to the 2022 MDS MSA diagnostic criteria; * all patients had been ruled out of polyQ disease by genetic testing; * Voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

* pregnancy or breastfeeding; * contraindications to MRI examination or inability to cooperate in completing neuroimaging examination; * previous history of other neurological disorders or presence of other organic intracranial lesions on neuroimaging that cannot be interpreted by MSA, such as epilepsy, trauma, tumors, or high-grade cerebral white matter degeneration (Fazekas grade 2 and above); * History of alcohol or drug abuse

Design outcomes

Primary

MeasureTime frame
Standard uptake value ratio(SUVR)From enrollment to the end of treatment at 4 weeks

Secondary

MeasureTime frameDescription
H-Y stageFrom enrollment to the end of treatment at 4 weeks
SCOPA-AUTFrom enrollment to the end of treatment at 4 weeksParkinson's Disease Autonomic Symptoms Scale
Wexner scoreFrom enrollment to the end of treatment at 4 weeksWexner Continence Grading Scale
UMSARSFrom enrollment to the end of treatment at 4 weeksUnified Multiple System Atrophy Rating Scale
MoCA scoreFrom enrollment to the end of treatment at 4 weeksMontreal Cognitive Assessment
TSPO Single nucleotide polymorphism genotypingFrom enrollment to the end of treatment at 4 weeks
Frontal Assessment BatteryFrom enrollment to the end of treatment at 4 weeks

Countries

China

Contacts

Primary ContactHe RQ 何
hrq1234562001@163.COM0086 186 2214 8869

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026